AU2003238211A1 - 1,6,9,14-tetrasubstituted terrylene tetracarboxylic acid diimides - Google Patents

1,6,9,14-tetrasubstituted terrylene tetracarboxylic acid diimides

Info

Publication number
AU2003238211A1
AU2003238211A1 AU2003238211A AU2003238211A AU2003238211A1 AU 2003238211 A1 AU2003238211 A1 AU 2003238211A1 AU 2003238211 A AU2003238211 A AU 2003238211A AU 2003238211 A AU2003238211 A AU 2003238211A AU 2003238211 A1 AU2003238211 A1 AU 2003238211A1
Authority
AU
Australia
Prior art keywords
substituted
alkyl
alkoxy
optionally
het
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
AU2003238211A
Other versions
AU2003238211A8 (en
Inventor
Arno Bohm
Matthias Krieger
Klaus Mullen
Erik Reuther
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Max Planck Gesellschaft zur Foerderung der Wissenschaften eV
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Publication of AU2003238211A8 publication Critical patent/AU2003238211A8/en
Publication of AU2003238211A1 publication Critical patent/AU2003238211A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/06—Peri-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
    • C09B5/62—Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Chemical And Physical Treatments For Wood And The Like (AREA)
  • Organic Insulating Materials (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Stringed Musical Instruments (AREA)

Abstract

New 1,6,9,14-tetra-substituted terrylenetetracarbodiimides (I) are claimed, in which the 1,6-positions and 9,14-positions independently are substituted by bromo, cyano, (het)aryloxy, (het)arylthio, optionally substituted (hetero)-alk(en)yl or -alkynyl, N-heterocyclyleth(en)yl, N-heterocyclylethynyl or (substituted) amino. 1,6,9,14-Tetra-substituted terrylenetetracarbodiimides of formula (I) are new X, Y = Br, CN, (het)aryloxy or (het)arylthio (optionally mono- or poly-substituted by 1-12C alkyl, 1-12C alkoxy, -COOR1, -SO3R1, halogen, COOH, carboxy, CN, -CONHR2 and/or -NHCOR2), -L-R3, -N(R2)2; R, R' = H, 1-30C alkyl (optionally with -O-, -S-, -NR1-, -CO- and/or -SO2- group(s) in the chain and optionally mono- or poly-substituted by CN, 1-6 C alkoxy, aryl (optionally substituted by 1-18 C alkyl or 1-6 C alkoxy) and/or a 5-7-N-heterocyclic group, which may contain other hetero-atoms and may be aromatic), 5-8 C cycloalkyl (optionally with -O-, -S- and/or -NR1- group(s) in the C skeleton and/or mono- or poly-substituted by 1-6 C alkyl), (het)aryl (optionally mono- or poly-substituted by 1-18 C alkyl, 1-6 C alkoxy, CN, -CONHR2, -NHCOR2 and/or (het)arylazo, which may be substituted by 1-10 C alkyl, 1-6 C alkoxy or CN); L = 1,2-ethylene, 1,2-ethenylene or 1,2-ethynylene; R1 = H or 1-6C alkyl; R2 = H, 1-18C alkyl or (het)aryl, optionally substituted by 1-6 C alkyl, 1-6 C alkoxy, halogen, OH, carboxy or CN); R3 = 1-18C alkyl (optionally with -O-, -S-, -NR1-, -CO- and/or -SO2- group(s) in the chain and optionally substituted by -COOR1, -SO3R1, OH, CN, 1-6C alkoxy, aryl (optionally substituted by 1-18 C alkyl or 1-6 C alkoxy) and/or a 5-7-N-heterocyclic group, which may contain other hetero-atoms and may be aromatic). Independent claims are also included for methods of preparing (I).
AU2003238211A 2002-06-07 2003-06-04 1,6,9,14-tetrasubstituted terrylene tetracarboxylic acid diimides Abandoned AU2003238211A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10225595.4 2002-06-07
DE10225595A DE10225595A1 (en) 2002-06-07 2002-06-07 New 1,6,9,14-tetra-substituted terrylenetetracarbodiimides, preparation and use as colorant, dispersant, pigment additive, intermediate, emitter and laser dye and in fluorescence conversion, bioluminescence array and photovoltaics
PCT/EP2003/005817 WO2003104232A1 (en) 2002-06-07 2003-06-04 1,6,9,14-tetrasubstituted terrylene tetracarboxylic acid diimides

Publications (2)

Publication Number Publication Date
AU2003238211A8 AU2003238211A8 (en) 2003-12-22
AU2003238211A1 true AU2003238211A1 (en) 2003-12-22

Family

ID=29557708

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2003238211A Abandoned AU2003238211A1 (en) 2002-06-07 2003-06-04 1,6,9,14-tetrasubstituted terrylene tetracarboxylic acid diimides

Country Status (9)

Country Link
US (1) US7521556B2 (en)
EP (1) EP1513841B1 (en)
JP (1) JP4532265B2 (en)
KR (1) KR101015478B1 (en)
CN (1) CN1318419C (en)
AT (1) ATE395347T1 (en)
AU (1) AU2003238211A1 (en)
DE (2) DE10225595A1 (en)
WO (1) WO2003104232A1 (en)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7145010B2 (en) * 2001-03-23 2006-12-05 Basf Aktiengesellschaft Tert-alkylphenoxy-substituted polycyclic compounds
CN1980791B (en) 2004-01-26 2012-08-22 西北大学 Perylene n-type semiconductors and related devices
DE102004018547A1 (en) 2004-04-14 2005-02-03 Basf Ag Welding plastics with invisible laser radiation, e.g. in packaging, uses visibly transparent, colorless, thermostable nonionic polycyclic organic compound, doped tin oxide or lanthanide or alkaline earth hexaboride as radiation absorber
DE102004048729A1 (en) * 2004-10-05 2006-04-06 Basf Ag Process for the preparation of halogenated rylenecarboximides
DE102004057585A1 (en) * 2004-11-29 2006-06-01 Basf Ag New rylene tetracarbonic acid diimide compounds useful e.g. for coloring high-molecular organic and inorganic materials; as dispersants; preparing aqueous polymer dispersions, markings and letters that absorb light from infra-red light
DE102005021362A1 (en) * 2005-05-04 2006-11-09 Basf Ag Terrylene and Quaterrylene Derivatives
DE102005032583A1 (en) * 2005-07-11 2007-01-25 Basf Ag Substituted Rylene Derivatives
DE102005037115A1 (en) * 2005-08-03 2007-02-08 Basf Ag polychromophores
DE102005043572A1 (en) * 2005-09-12 2007-03-15 Basf Ag Fluorescence conversion solar cells based on terrylene fluorescent dyes
JP2009528277A (en) 2006-02-17 2009-08-06 ビーエーエスエフ ソシエタス・ヨーロピア Fluorinated rylenetetracarboxylic acid derivatives and their use
EP1843407A1 (en) 2006-04-07 2007-10-10 Basf Aktiengesellschaft Liquid crystalline rylenetetracarboxylic acid derivatives and their use
US20070259475A1 (en) * 2006-05-04 2007-11-08 Basf Aktiengesellschaft Method for producing organic field-effect transistors
KR101364873B1 (en) * 2006-05-04 2014-02-19 바스프 에스이 Method for producing organic field-effect transistors
US7569693B2 (en) * 2006-06-12 2009-08-04 Northwestern University Naphthalene-based semiconductor materials and methods of preparing and use thereof
WO2008051552A2 (en) * 2006-10-25 2008-05-02 Northwestern University Organic semiconductor materials and methods of preparing and use thereof
JP5380296B2 (en) * 2006-11-17 2014-01-08 ポリエラ コーポレイション Diimide-based semiconductor material and method for preparing and using diimide-based semiconductor material
WO2008085942A2 (en) * 2007-01-08 2008-07-17 Polyera Corporation Methods for preparing arene-bis(dicarboximide)-based semiconducting materials and related intermediates for preparing same
US8022214B2 (en) * 2007-01-24 2011-09-20 Polyera Corporation Organic semiconductor materials and precursors thereof
WO2008113753A1 (en) * 2007-03-16 2008-09-25 Basf Se Method for the production of rylene tetracarboxylic acid diimides the imide nitrogens of which carry hydrogen atoms and the use thereof
DE102007015261A1 (en) 2007-03-27 2008-10-02 Aacure Aadhesives Gmbh Reactive mass for substrate application, preferably for the generation of a glop-top, comprises a thermally initiable matrix forming material and an energy absorbing initiator, where the initiator is soluble in the reactive mass
WO2009000831A1 (en) * 2007-06-25 2008-12-31 Basf Se Bromine-substituted rylene tetracarboxylic acid derivatives, and the use thereof
KR20160029863A (en) * 2008-02-05 2016-03-15 바스프 에스이 Perylene semiconductors and methods of preparation and use thereof
WO2009141288A2 (en) * 2008-05-19 2009-11-26 Basf Se Switchable special effect substances
DE102011007196A1 (en) 2011-04-12 2012-10-18 Evonik Degussa Gmbh Producing a composite part contains joint partner including molded part made of a polyamide molding composition and a molded part made of a methacrylate copolymer molding composition comprising e.g. 2-methyl-propionic acid methyl ester
AR086509A1 (en) * 2011-05-25 2013-12-18 Sicpa Holding Sa DYES OF QUATERRYLENE AND / OR LAND UNITED TO POLYMERS AND COMPOSITIONS CONTAINING THEM
CN104674348B (en) * 2013-12-02 2017-05-10 济南大学 Method for preparing zinc sulfide/amphiphilic perylene bisimide hybrid semiconductor material with different crystal phases
CN113613496A (en) 2019-03-22 2021-11-05 巴斯夫欧洲公司 Plant cultivation method
EP3858946A1 (en) 2020-01-29 2021-08-04 Basf Se New rylene dicarboximides
DE102021132512A1 (en) 2021-12-09 2023-06-15 OSRAM Opto Semiconductors Gesellschaft mit beschränkter Haftung OPTOELECTRONIC DEVICE AND METHOD FOR MANUFACTURING OPTOELECTRONIC DEVICE
WO2023105029A1 (en) * 2021-12-09 2023-06-15 Basf Se Terrylene diimide and quaterrylene diimide colorants

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10039232A1 (en) * 2000-08-11 2002-02-21 Basf Ag Liquid crystalline perylene-3,4: 9,10-tetracarboxylic acid diimides
DE10039643A1 (en) * 2000-08-14 2002-02-28 Max Planck Gesellschaft Functionalized perylene tetracarboxylic acid diimides
US7145010B2 (en) * 2001-03-23 2006-12-05 Basf Aktiengesellschaft Tert-alkylphenoxy-substituted polycyclic compounds

Also Published As

Publication number Publication date
US7521556B2 (en) 2009-04-21
KR101015478B1 (en) 2011-02-22
JP4532265B2 (en) 2010-08-25
DE50309848D1 (en) 2008-06-26
KR20050013567A (en) 2005-02-04
DE10225595A1 (en) 2003-12-18
US20050222416A1 (en) 2005-10-06
AU2003238211A8 (en) 2003-12-22
CN1659167A (en) 2005-08-24
EP1513841A1 (en) 2005-03-16
WO2003104232A1 (en) 2003-12-18
ATE395347T1 (en) 2008-05-15
EP1513841B1 (en) 2008-05-14
CN1318419C (en) 2007-05-30
JP2005531610A (en) 2005-10-20

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Legal Events

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MK6 Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase
TH Corrigenda

Free format text: IN VOL 18, NO 7, PAGE(S) 1718 UNDER THE HEADING APPLICATIONS OPI - NAME INDEX UNDER THE NAME BASF AKTIENGESELLSCHAFT, APPLICATION NO. 2003238211, UNDER INID (71) CORRECT THE NAME TO READ MAX-PLANCK-GESELLSCHAFT ZUR F#RDERUNG DER WISSENSCHAFTEN E.V.; BASF AKTIENGESELLSCHAFT